Lead development and execution of medical marketing initiatives for DT120 commercial launch
Drive KOL engagement, advisory boards, and medical congress strategies
Synthesize insights and lead scientific communication materials to support launch readiness
Definium Therapeutics is a late-stage clinical biopharmaceutical company applying scientific rigor to psychedelics to develop treatments for psychiatric and neurological disorders. Headquartered in New York and publicly traded on Nasdaq, the company fosters a culture of relentless innovation and collaboration to move psychiatry forward.
Serve as primary point-of-contact liaison with clients and oversee all aspects of clinical trials.
Manage study budgets, project timelines, risk, and cross-functional teams to ensure quality and compliance.
Drive bid defense preparation, client presentations, and continuous process improvement across assigned portfolios.
Precision for Medicine supports clinical research and development for biopharmaceutical and life science companies. It is a global, collaborative organization that emphasizes quality, innovation, and professional growth.
Establish, grow, and lead the national field-based MSL team, defining operational frameworks and best practices.
Oversee field-based support of clinical trials and strategic engagement of key thought leaders.
Ensure high standards of scientific excellence and compliance with all applicable regulations.
Orca Bio is a commercial-stage biotechnology company redefining the transplant process by developing next-generation cell therapies for blood cancer patients. With a small, entrepreneurial team, they maintain a start-up culture of camaraderie and leadership by example.
Lead and manage the assigned clinical operations team, setting and executing departmental strategy.
Oversee clinical trial agreements, budgets, and the timely execution of clinical research programs from conception through final study report.
Maintain oversight of study conduct at sites, ensure adherence to protocols and GCP, and serve as company representative at external meetings.
Iovance Biotherapeutics is the global leader in innovating, developing, and delivering tumor infiltrating lymphocyte (TIL) cell therapies for patients with solid tumors. As an end-to-end cell therapy company with fully owned, centralized U.S.-based manufacturing, it operates with a fast-paced, collaborative culture focused on bringing first-in-class treatments to cancer patients.
Provide strategic medical leadership for clinical safety across investigational therapies for pulmonary fibrosis.
Conduct hands-on medical review of serious adverse events and lead signal detection and benefit-risk assessments.
Oversee cross-functional safety review meetings and regulatory interactions.
The company is a clinical-stage biotechnology firm developing innovative therapies for pulmonary fibrosis and other serious respiratory diseases. It is a growing, lean organization with a focus on pharmacovigilance infrastructure and global clinical development.
Lead, coach, and develop Field Medical teams to deliver high-quality, compliant scientific engagement in oncology.
Translate medical and therapeutic area strategy into regional field priorities and execution plans.
Partner with Medical Affairs leadership and cross-functional teams to align regional field activity with medical objectives.
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. It is a global biopharmaceutical company focused on immunology, oncology, neuroscience, and aesthetics, with a culture of integrity, innovation, and community.
Lead full service clinical projects in Oncology, ensuring timelines, budget, and quality.
Serve as primary client liaison and coordinate cross-functional teams across all study stages.
Manage all aspects of clinical trials, including proposal strategy, documentation, and reporting.
Precision for Medicine is a CRO enabling precision medicine through novel clinical trial designs, biomarker and data analytics, and a focus on rare diseases and oncology. We are a supportive, collaborative team that values work life balance and development.
Lead medical writing for one or more clinical programs and drive content strategy for clinical and regulatory documents.
Author and manage high-quality clinical study protocols, investigator's brochures, clinical study reports, and global regulatory submissions.
Collaborate cross-functionally, mentor direct reports, and incorporate process improvements to support R&D needs.
Deciphera is a biopharmaceutical company dedicated to developing innovative medicines for people living with cancer. They value diversity and offer a competitive compensation and benefits package, fostering a culture of collaboration and professional growth.
Serve as the primary field-based scientific expert engaging healthcare professionals to exchange clinical and research knowledge.
Build and maintain scientific relationships with HCPs, professional societies, and healthcare organizations in the Northern California territory.
Support clinical development, deliver training, and represent Sobi at medical conferences.
Sobi is a specialized biopharmaceutical company dedicated to developing and delivering innovative therapies for rare diseases. With over 1,900 employees in more than 30 countries, the company fosters a collaborative, inclusive culture focused on making a difference for patients.
Translate Medical Affairs priorities into actionable content strategies and clear creative briefs.
Develop or guide medical copy, messaging, and concepts while providing strategic direction to production teams.
Establish content guidelines and governance frameworks to ensure consistency across channels and activations.
Indegene is a technology-led healthcare solutions provider that enables healthcare organizations to be future ready. We are a rapidly growing global organization celebrating entrepreneurship and guided by passion, innovation, collaboration, and empathy.
Direct and manage a team of Project Directors and Project Managers in global project delivery.
Provide leadership and oversight for clinical programs and act as primary escalation point for sponsors.
Optimize profitability, manage resources, and ensure compliance with quality standards and regulations.
Precision Medicine Group provides clinical research and project management services for global clinical trials. The company promotes a culture centered on quality, people, clients, and performance.
Serve as a TIL cell therapy expert in Medical Affairs, educating providers and optimizing tumor tissue procurement.
Lead engagement with surgeons and cross-functional teams to support clinical trials and medical strategy.
Represent Iovance at professional meetings and contribute to publications and educational materials.
Iovance Biotherapeutics is a global leader in developing tumor infiltrating lymphocyte (TIL) cell therapies for solid tumors. It is an end-to-end cell therapy company with U.S.-based manufacturing and an inclusive culture.
Own the Field Excellence operating model nationally, including cadence, standards, tools, and escalation protocols.
Serve as the single operational partner to the VP Sales, managing territory, IC questions, and business review preparation.
Manage and develop two Directors of Field Excellence and ensure launch readiness across all geographies.
Summit Therapeutics is a biopharmaceutical oncology company focused on improving quality of life and resolving serious unmet medical needs through clinical studies. The company is building its commercial infrastructure for a first US launch, with a mission-driven culture emphasizing integrity, collaboration, and commitment to people.
Conduct peer-to-peer educational programs for advanced practice providers and nurses on Legend cell therapy products.
Collaborate with sales, marketing, and cross-functional teams to deliver on-label education and support regional initiatives.
Build relationships with key nurse opinion leaders and provide training on disease management and adverse event identification.
Legend Biotech is a global biotechnology company dedicated to treating and curing life-threatening diseases through innovative cell therapies. It partners with Johnson & Johnson to develop and commercialize CARVYKTI® and is committed to discovering safe, effective therapies for patients worldwide.
Leads and develops a team of Medical Directors and Clinical Directors driving clinical strategy across enterprise value-based care contracts.
Owns clinical performance outcomes, resource deployment, and strategic market relationships.
Recruits and mentors clinical leaders while representing the clinical voice in company-wide strategy.
Aledade PBC is a public benefit corporation that empowers independent primary care practices by building value-based care contracts and technology. Founded in 2014, it is the largest network of independent primary care in the U.S. and fosters a collaborative, inclusive, remote-first culture.
Provide statistical leadership for oncology clinical development programs, including Phase I–III trials and regulatory submissions.
Lead development of SAPs, sample size calculations, randomization strategies, and ensure quality of statistical deliverables.
Collaborate with cross-functional teams, serve as statistical SME, and mentor junior biostatisticians.
ClinChoice is a global full-service CRO delivering clinical development and functional solutions for pharmaceutical, biotechnology, and medical device companies. With over 4,000 professionals in 20+ countries, we are committed to high-quality delivery, continuous training, and a diverse, inclusive culture.
Lead a team of seven CAEs in the Northeast to drive patient impact through exceptional customer engagement and key account management.
Develop people via coaching, feedback, and career development, translating strategy into purposeful execution.
Manage budgets and resources to maximize patient impact and foster a high-performance culture.
AbbVie discovers and delivers innovative medicines and solutions across immunology, oncology, neuroscience, and aesthetics. It is a global biopharmaceutical company with a culture focused on integrity, innovation, and making a remarkable impact on patients' lives.
Serve as a core medical expert in precision medicine and cancer genomics, supporting real-world evidence and custom data requests.
Collaborate with cross-functional teams and biopharma clients across the R&D lifecycle, from discovery to post-market development.
Apply clinical development and trial design principles to bridge traditional endpoints with real-world data for external control arms.
Flatiron Health is a healthcare technology company reimagining the infrastructure of cancer care by leveraging real-world evidence and data analytics. It values integrity, inspires growth, and is building a modern, connected oncology ecosystem.
Serve as primary medical and scientific expert for clinical trial protocols and Expanded Access Programs.
Monitor trials to ensure participant safety, data accuracy, and protocol compliance.
Lead protocol development, investigator training, and cross-functional collaboration.
WEP Clinical partners with biopharmaceutical sponsors to deliver clinical trials, expanded access programs, and market access solutions. With 15+ years of experience across 150+ countries, they offer operational scale and a personalised culture.
Establish and maintain peer relationships with key opinion leaders and act as the primary clinical/scientific resource to healthcare providers.
Support evidence generation initiatives, identify gaps in research, and report medical insights to inform strategy.
Attend medical conferences, respond to scientific requests, and ensure compliance with FDA regulations and company policies.
Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led by physician-scientists for over 30 years, it has an award-winning culture and has produced multiple FDA-approved treatments.